Labshake search
Citations for Illumina :
2401 - 2450 of 10000+ citations for Creatinine Serum Low Sample Volume Kit 384 well Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Cancer Biology 2020Quote: ... Samples were sequenced (HiSeq 4000 instrument, Illumina Inc) in paired-end mode on Illumina (2×101 bp ...
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bioRxiv - Developmental Biology 2020Quote: Samples were then circularized with CircLigase (Illumina, CL4115K) in a 20 μL reaction (15 μL cDNA ...
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bioRxiv - Immunology 2021Quote: ... Samples were scanned using the iScan system (Illumina). Subsequently ...
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bioRxiv - Genetics 2020Quote: ... Samples were sequenced on a HiSeq2500 HighOutput (Illumina) with a 5% spike-in of PhiX.
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bioRxiv - Neuroscience 2022Quote: ... The samples were sequenced using NGS (Illumina HiSeq3000) at an average of ∼15 million paired-end reads per sample.
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bioRxiv - Cancer Biology 2022Quote: ... Samples were sequenced on a HiSeq2500 HighOutput (Illumina) with a 5% spike-in of PhiX ...
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bioRxiv - Genetics 2022Quote: ... samples were sequenced on one NovaSeq 6000 (Illumina) S4 PE150 flowcell ...
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bioRxiv - Molecular Biology 2022Quote: ... Samples were sequenced on the HiSeq 2500 (Illumina) platform with a read depth of approximately 7.6 million reads (single-end 100 bp reads ...
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bioRxiv - Microbiology 2022Quote: Sample demultiplexing was performed using bcl2fastq 2.20.0 (Illumina), and quality and adapter trimming of reads was performed using Cutadapt 2.8 (28) ...
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bioRxiv - Molecular Biology 2022Quote: ... Samples were sequenced in a MiSeq Nano (Illumina) with 10 % of PhiX spike-in ...
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bioRxiv - Bioengineering 2022Quote: ... All samples were sequenced on the NextSeq500 (Illumina) in midoutput mode producing 160 million paired end 75 bp reads ...
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Group B Streptococcus Adaptation Promotes Survival in a Hyperinflammatory Diabetic Wound EnvironmentbioRxiv - Microbiology 2022Quote: ... Samples were rRNA depleted using RiboZero Plus (Illumina) and libraries for the 12 mouse samples and 3 input bacteria cDNA samples were sequenced using the Illumina Stranded RNA sequencing platform ...
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bioRxiv - Cancer Biology 2022Quote: ... The samples were sequenced on HiSeq 2000 (Illumina), and 30-50 million paired-end reads from each sample were recorded.
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bioRxiv - Cell Biology 2024Quote: ... Samples were sequenced with a NextSeq 500 (Illumina) using 75bp single-end reads ...
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bioRxiv - Cell Biology 2023Quote: ... Samples were sequenced by NovaSeq 6000 System (Illumina) at the Weill Cornell Medicine ...
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bioRxiv - Genomics 2023Quote: ... Samples were sequenced on a HiSeq2500 HighOutput (Illumina) with a 5% spike-in of PhiX ...
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bioRxiv - Genomics 2023Quote: ... Samples were then pooled and sequenced by Illumina NovaSeq (90.4-103.9M ...
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bioRxiv - Neuroscience 2022Quote: ... Samples were sequenced on a Next-seq (Illumina) at the Johns Hopkins University Single Cell and Transcriptomics Sequencing Core.
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bioRxiv - Immunology 2023Quote: ... Samples were sequenced on a HiSeq 2500 (Illumina).
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bioRxiv - Cell Biology 2023Quote: ... Samples were sequenced on a NextSeq 2000 (Illumina).
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bioRxiv - Cancer Biology 2023Quote: ... Samples were sequenced on the NovaSeq 6000 (Illumina) with paired end index read and the TruSeq v2 library.
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bioRxiv - Genomics 2023Quote: ... Samples were sequenced on a HiSeq2500 HighOutput (Illumina) with a 5% spike-in of PhiX ...
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bioRxiv - Cell Biology 2023Quote: ... Samples were sequenced using a NextSeq 5000 (Illumina) in the same flow cell and were pulled equimolarly.
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bioRxiv - Cancer Biology 2023Quote: ... Samples were hybridized with Ribo-Zero Gold (Illumina) to deplete cytoplasmic and mitochondrial rRNA ...
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bioRxiv - Genomics 2023Quote: ... Samples were sequenced on a NovaSeq 6000 (Illumina) to reach approximately 25M paired-end reads per sample.
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bioRxiv - Microbiology 2023Quote: ... Samples were loaded onto a MiSeq NanoCell (Illumina) and paired-end RNA sequencing was performed on a NovaSeq 6000 sequencing platform (Illumina) ...
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bioRxiv - Immunology 2022Quote: ... Samples were sequenced using the NovaSeq 6000 (Illumina) in paired-end mode ...
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bioRxiv - Genetics 2023Quote: ... Samples were sequenced on a MiSeq instrument (Illumina) with 2×76bp paired-end reads ...
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bioRxiv - Immunology 2023Quote: ... Samples were run on a NovaSeq 6000 (Illumina). An average of 64 million paired reads were generated per sample ...
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bioRxiv - Cancer Biology 2023Quote: ... Samples were sequenced on a NovaSeq 6000 (Illumina).
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bioRxiv - Cell Biology 2023Quote: ... Samples were then sequenced using a MiSqeq (Illumina) and alignment of NGS results to the genome was performed using SerialCloner software with allele specific reads reported at approximately a 50:50 ratio ...
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bioRxiv - Molecular Biology 2023Quote: ... Samples were sequenced on a NextSeq 550 (Illumina) system using a NextSeq 500/550 Mid Output v2.5 (75 Cycles ...
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bioRxiv - Neuroscience 2023Quote: ... Base call files for each sample from Illumina were demultiplexed into FASTQ reads ...
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bioRxiv - Immunology 2023Quote: ... Samples were sequenced on HI-Seq 2500 (Illumina). 11 nucleotide adaptors were trimmed from each read and resultant sequences were aligned to the mm10 genome using bowtie2 (Langmead and Salzberg ...
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bioRxiv - Genetics 2024Quote: ... DNA samples for GWA6 were genotyped by Illumina Global Screen Array (https://www.illumina.com/products/by-type/microarray-kits/infinium-global-screening.html) ...
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bioRxiv - Neuroscience 2024Quote: ... Base call files for each sample from Illumina were demultiplexed into FASTQ reads ...
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CTCF regulates global chromatin accessibility and transcription during rod photoreceptor developmentbioRxiv - Genomics 2024Quote: ... All samples were sequenced with NovaSeq 6000 (Illumina) at the NHLBI Genomics Core Facility by 50 bp paired-end sequencing.
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bioRxiv - Molecular Biology 2024Quote: ... The samples were sequenced on HiSeq 2500 (Illumina) and NovaSeq 6000 (Illumina ...
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bioRxiv - Molecular Biology 2024Quote: ... The samples were sequenced on HiSeq 2500 (Illumina) and NovaSeq 6000 (Illumina ...
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bioRxiv - Molecular Biology 2024Quote: The sample for next-generation sequencing (Illumina MiSeq) were prepared by PCR amplification using a primer pair (Table S1 ...
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bioRxiv - Cancer Biology 2024Quote: ... Samples were sequenced on a NextSeq 2000 (Illumina) with 30 million 2×100bp paired end reads by the Glasgow Polyomics next generation sequencing and transcriptomics service.
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bioRxiv - Neuroscience 2024Quote: ... Samples were sequenced on a Nova-seq (Illumina) at the Johns Hopkins University Single Cell and Transcriptomics Sequencing Core at a minimum read depth of 50000 reads per nucleus.
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bioRxiv - Developmental Biology 2024Quote: ... Samples were demultiplexed using bcl2fastq Conversion Software (Illumina). Adaptor trimmed FASTQ paired- end reads were aligned using STAR (v.2.6.1a ...
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bioRxiv - Cancer Biology 2023Quote: ... The library preparation for bulk tumors and cell lines was generated using the TruSeq Stranded mRNA sample preparation kit (Illumina Inc., San Diego, RS-122-2101/2) according to the manufacturer’s instructions (Illumina ...
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bioRxiv - Developmental Biology 2024Quote: ... we prepared n=40 sequencing libraries from 1µg total RNA per sample using Illumina® Stranded mRNA Prep kits with unique 5′ and 3′ index adapter pairs (IDT for Illumina® RNA UD Indexes, Set A). Libraries were PCR amplified for 10 cycles ...
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bioRxiv - Plant Biology 2023Quote: ... as per manufacturer’s instructions except that reaction volumes were scaled by one-half and 12 PCR cycles were used for library amplification (Illumina, San Diego, California, USA). Paired-end sequencing (2 × 150 bp ...
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bioRxiv - Genomics 2019Quote: ... a state-of-the-art method for calling low allele frequency variants in deep sequencing data (although originally designed to detect sub-clonal mutations on Illumina rather than Ion AmpliSeq data). We run deepSNV (version 1.21.3 ...
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bioRxiv - Molecular Biology 2023Quote: ... and each sample was sequenced in 3 different lanes (3 technical replicates per sample) on an Illumina HiSeq platform (Illumina, USA).
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bioRxiv - Cell Biology 2023Quote: ... and 5-day deligated samples were sequenced (the ligated sample was sequenced on the Illumina Nextseq500 and all others were sequenced on the Illumina Nextseq2000), and initial processing of the datasets was performed at the Center for Functional Genomics at the University at Albany ...
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bioRxiv - Molecular Biology 2020Quote: ... Each well was mixed with 0.8 μl Nextera tagmentation DNA buffer (Illumina) and 0.4 μl Tn5 enzyme (Illumina) ...